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Merck

62139

Sigma-Aldrich

(-)-芳樟醇

≥95.0% (sum of enantiomers, GC)

别名:

(R)-(-)-3,7-二甲基-1,6-辛二烯-3-醇

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About This Item

线性分子式:
(CH3)2C=CHCH2CH2C(CH3)(OH)CH=CH2
CAS号:
分子量:
154.25
Beilstein:
1721487
EC號碼:
MDL號碼:
分類程式碼代碼:
12352002
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

≥95.0% (sum of enantiomers, GC)

光學活性

[α]20/D −18±3°, neat

折射率

n20/D 1.4615 (lit.)
n20/D 1.462

bp

198 °C (lit.)

密度

0.862 g/mL at 20 °C (lit.)

官能基

hydroxyl

SMILES 字串

C\C(C)=C\CC[C@@](C)(O)C=C

InChI

1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3/t10-/m0/s1

InChI 密鑰

CDOSHBSSFJOMGT-JTQLQIEISA-N

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一般說明

(-)-芳樟醇是一种单萜化合物,主要存在于许多精油中。它具有抗伤害和抗炎活性。

應用

(-)-芳樟醇可用作反应物参与:
  • 通过非对映选择性自由基级联环化,对映选择性地制备蛇孢假壳素二倍半萜
  • 通过 (-)-里哪醇O-三乙基甲硅烷醚进行(-)-5,6-二氢霉素B 的全合成
  • pladienolide B 类似物的全合成

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

166.3 °F - closed cup

閃點(°C)

74.6 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Amy L Parachnowitsch et al.
Plant signaling & behavior, 8(1), e22704-e22704 (2012-12-12)
Natural selection is thought to have shaped the evolution of floral scent; however, unlike other floral characters, we have a rudimentary knowledge of how phenotypic selection acts on scent. We found that floral scent was under stronger selection than corolla
Synthesis of a pladienolide B analogue with the fully functionalized core structure
Mu?ller S, et al.
Organic Letters, 13(15), 3940-3943 (2011)
Nan Zhang et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 23(14), 1727-1734 (2016-12-04)
Essential oil from Cananga odorata (ylang-ylang essential oil, YYO) is usually used in reducing blood pressure, improving cognitive functioning in aromatherapy in human. Few reports showed its effect on anxiety behaviors. To investigate the anxiolytic effects of YYO exposure on
(-)-Linalool produces antinociception in two experimental models of pain.
Peana AT, et al.
European Journal of Pharmacology, 460(1), 37-41 (2003)
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Microbial cell factories, 20(1), 54-54 (2021-03-04)
Linalool, an acyclic monoterpene alcohol, is extensively used in the flavor and fragrance industries and exists as two enantiomers, (S)- and (R)-linalool, which have different odors and biological properties. Linalool extraction from natural plant tissues suffers from low product yield.

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